Author

B. Picatoste

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Physiology· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:mouse· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Approach:genetic perturbation / CRISPR· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

L. Yammine· 2 shared R. Leahey· 2 shared T. E. McGraw· 2 shared A. Garcia-Ocana· 1 shared C. Rosselot· 1 shared D. Soares· 1 shared J. C. Lo· 1 shared J. Wen· 1 shared

Activity by Year

2020-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersPhysiology

L. Yammine

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2 papers

Recent·Most cited

Blunting of insulin-stimulated glucose uptake in brown adipose tissue induces systemic metabolic dysregulation in female mice

B. Picatoste, L. Yammine, R. Leahey, D. Soares, P. Cohen, T. E. McGraw

This study shows that reducing glucose uptake in brown adipose tissue in female mice leads to systemic metabolic issues, independent of thermogenesis.

bioRxiv · Dec 9, 2020 · PreprintPhysiology

Spatiotemporal regulation of GIPR signaling impacts glucose homeostasis as revealed in studies of a common GIPR variant.

L. Yammine, B. Picatoste, N. Abdullah, R. Leahey, N. Gomez-Banoy, C. Rosselot, J. Wen, M. D. Goncalves, J. C. Lo, A. Garcia-Ocana, T. E. McGraw

This study investigates the impact of a GIPR variant on glucose homeostasis using a mouse model, finding altered intracellular trafficking and increased GIP sensitivity.

bioRxiv · May 12, 2020Physiology